Аннотация:
Eight novel aza-14-crown-4 compounds incorporating γ-arylpyridine moiety and possessing high inhibitory activity towards cancer cell lines were synthesized in one step from 1,5-bis(2-acetylphenoxy)-3-oxapentane, aromatic aldehyde and ammonium acetate.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
A. T. Le, H. H. Truong, T. Thi, N. Thi, H. To, H. Thi, A. T. Soldatenkov, “Synthesis and biological activity of (γ-arylpyridino)-dibenzoaza-14-crown-4 ethers”, Mendeleev Commun., 25:3 (2015), 224–225
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2359
https://www.mathnet.ru/rus/mendc/v25/i3/p224
Эта публикация цитируется в следующих 21 статьяx:
V. T. Tran, N. T. Dao, T. T. Do, T. T. Pham, D. T. Le, V. N. Khrustalev, Ph. T. Nguyen, A. T. Le, “New pyridine dithiaazacrown ether derivatives: synthesis, structural characterization, in silico and in vitro biological studies”, Mendeleev Commun., 34:4 (2024), 514–517
Mohit B. Patel, Helena Spikes, Robert S. Bailey, Thomas Connell, Hannah Gill, Michael R. Gokel, Rebecca Harris, Joseph W. Meisel, Saeedeh Negin, Shanheng Andrew Yin, George W. Gokel, “Antimicrobial and Adjuvant Potencies of Di-n-alkyl Substituted Diazalariat Ethers”, Antibiotics, 12:10 (2023), 1513
D. T. Nguyen, H. H. Truong, N. T. Dao, V. T. Tran, O. S. Gorchakova, A. T. Le, “Unexpected hydrazine- and hydroxylamine-induced transformations of aza-14-crown-4 incorporating 4-oxopiperidine-3-carboxylate moiety”, Mendeleev Commun., 33:5 (2023), 708–710
N. T. Dao, T. T. Do, T. T. Pham, V. T. Tran, V. N. Khrustalev, A. T. Le, “Molecular structure and ultrasound-assisted synthesis of the diazacrown derivative containing 2,3,4,6-tetraaryl-γ piperidone”, Mendeleev Commun., 33:5 (2023), 711–713
Faiz Ullah, Taskin Aman Khan, Jawaria Iltaf, Saleha Anwar, Muhammad Farhan Ali Khan, Muhammad Rizwan Khan, Sami Ullah, Muhammad Fayyaz ur Rehman, Muhammad Mustaqeem, Katarzyna Kotwica-Mojzych, Mariusz Mojzych, “Heterocyclic Crown Ethers with Potential Biological and Pharmacological Properties: From Synthesis to Applications”, Applied Sciences, 12:3 (2022), 1102
Nhung T. Dao, Victor N. Khrustalev, Elena I. Polyakova, Anh T. Le, “Synthesis and Biological Evaluation of Azacrownophanes Containing Tetrahydropyridine or Piperidone Subunits”, ChemistrySelect, 7:48 (2022)
Thanh Van Tran Thi, Manh Linh Nguyen, Tien Dat Nguyen, The Duan Le, Hong Hieu Truong, Victor N. Khrustalev, Tuan Anh Le, “Synthesis of the First Dithiaaza-17-Crown-5 Ethers Containing Piperidin-4-One Subunit”, Chem Heterocycl Comp, 57:10 (2021), 1057
Ayalew T. Wodajo, Thi Thanh Van Tran, Hong Hieu Truong, Alexander G. Tskhovrebov, The Duan Le, Victor N. Khrustalev, Tuan Anh Le, “Synthesis by deamination reaction and crystal structure at 120 K of (16Z,19E)-18-oxo-N-(pyridin-2-yl)-6,7,9,10-tetrahydro-18H-dibenzo[h,o][1,4,7]trioxacyclohexadecine-17-carboxamide”, Acta Crystallogr E Cryst Commun, 76:9 (2020), 1454
L. M. Nguyen, H. H. Truong, V. N. Khrustalev, S. T. Truong, D. T. Nguyen, V. T. Tran, S. T. Mai, V. T. Tran, A. T. Le, “Synthesis and biological evaluation of novel phane-structured diazacrowns containing γ-piperidone and pyridine rings”, Mendeleev Commun., 30:6 (2020), 753–755
А. Д. Зубенко, О. А. Фёдорова, “Ароматические и гетероароматические азакраун-соединения: преимущества и недостатки жестких макроциклических лигандов”, Усп. хим., 89:7 (2020), 750–786; A. D. Zubenko, O. A. Fedorova, “Aromatic and heteroaromatic azacrown compounds: advantages and disadvantages of rigid macrocyclic ligands”, Russian Chem. Reviews, 89:7 (2020), 750–786
Oscar Abelardo Ramírez-Marroquín, María Adelina Jiménez-Arellanes, Abimelek Cortés-Pacheco, Oscar R. Zambrano-Vásquez, Adolfo López-Torres, “Synthesis and in vivo anti- or pro-inflammatory activity of new bisphosphonates and vinylphosphonates”, Monatsh Chem, 150:2 (2019), 267
Thi Nhung Dao, Hong Hieu Truong, Van Boi Luu, Anatoly T. Soldatenkov, Nadezhda M. Kolyadina, Alena N. Kulakova, Victor N. Khrustalev, Ayalew T. Wodajo, Hong Quan Nguyen, Thi Tan Van Tran, Tuan Anh Le, “Synthesis and bioactivity of novel (γ-piperidono)dibenzo-33-aza-14-crown-3 ethers”, Chem Heterocycl Comp, 55:7 (2019), 654
A. T. Le, N. T. Dao, H. H. Truong, T. T. Do, E. I. Polyakova, I. V. Lin'ko, P. V. Dorovatovskii, V. N. Khrustalev, “Unexpected formation of dinaphthoaza-17-crown-5 ether containing γ-aminopiperidine subunit”, Mendeleev Commun., 29:6 (2019), 698–699
A. T. Le, V. T. Tran, H. H. Truong, L. M. Nguyen, D. M. Luong, T. T. Do, D. T. Nguyen, N. T. Dao, D. T. Le, A. T. Soldatenkov, V. N. Khrustalev, “Synthesis and cytotoxicity of novel γ-piperidone-containing dibenzo-1,7-diaza-14-crown-4 ethers”, Mendeleev Commun., 29:4 (2019), 375–377
Van Tuyen Nguyen, Hong Hieu Truong, Tuan Anh Le, Anatoly T. Soldatenkov, Tuyet Anh Dang Thi, Thi Thanh Van Tran, Natalia Ya. Esina, Victor N. Khrustalev, “Crystal structure of 22,24,25-trimethyl-8,11,14-trioxa-25-azatetracyclo[19.3.1.02,7.015,20]pentacosa-2,4,6,15(20),16,18-hexaen-23-one”, Acta Crystallogr E Cryst Commun, 73:2 (2017), 118
G.W. Gokel, S. Negin, R. Cantwell, Comprehensive Supramolecular Chemistry II, 2017, 3
T. Thanh Van Tran, Le Tuan Anh, Hung Huy Nguyen, Hong Hieu Truong, Anatoly T. Soldatenkov, “Crystal structure of 26-(4-methylphenyl)-8,11,14,17-tetraoxa-28-azatetracyclo[22.3.1.02,7.018,23]hexacosa-2,4,6,18(23),19,21,24(1),25,27-nonaene”, Acta Crystallogr E Cryst Commun, 72:5 (2016), 663
Saeedeh Negin, Mohit B. Patel, Michael R. Gokel, Joseph W. Meisel, George W. Gokel, “Antibiotic Potency against E. coli Is Enhanced by Channel‐Forming Alkyl Lariat Ethers”, ChemBioChem, 17:22 (2016), 2153
Anh Tuan Le, Anatoly T. Soldatenkov, “Strategies and methods for the synthesis of pyridinocrownophanes (microreview)”, Chem Heterocycl Comp, 52:3 (2016), 152
Mohit B. Patel, Evan C. Garrad, Ariel Stavri, Michael R. Gokel, Saeedeh Negin, Joseph W. Meisel, Zachary Cusumano, George W. Gokel, “Hydraphiles enhance antimicrobial potency against Escherichia coli, Pseudomonas aeruginosa, and Bacillus subtilis”, Bioorganic & Medicinal Chemistry, 24:12 (2016), 2864